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PGMD/curcumin nanoparticles for the treatment of breast cancer.

Abstract
The present study aims at developing PGMD (poly-glycerol-malic acid-dodecanedioic acid)/curcumin nanoparticles based formulation for anticancer activity against breast cancer cells. The nanoparticles were prepared using both the variants of PGMD polymer (PGMD 7:3 and PGMD 6:4) with curcumin (i.e. CUR NP 7:3 and CUR NP 6:4). The size of CUR NP 7:3 and CUR NP 6:4 were found to be ~ 110 and 218 nm with a polydispersity index of 0.174 and 0.36, respectively. Further, the zeta potential of the particles was - 18.9 and - 17.5 mV for CUR NP 7:3 and CUR NP 6:4, respectively. The entrapment efficiency of both the nanoparticles was in the range of 75-81%. In vitro anticancer activity and the scratch assay were conducted on breast cancer cell lines, MCF-7 and MDA-MB-231. The IC50 of the nanoformulations was observed to be 40.2 and 33.6 μM at 48 h for CUR NP 7:3 and CUR NP 6:4, respectively, in MCF-7 cell line; for MDA-MB-231 it was 43.4 and 30.5 μM. Acridine orange/EtBr and DAPI staining assays showed apoptotic features and nuclear anomalies in the treated cells. This was further confirmed by western blot analysis that showed overexpression of caspase 9 indicating curcumin role in apoptosis.
AuthorsMankamna Kumari, Nikita Sharma, Romila Manchanda, Nidhi Gupta, Asad Syed, Ali H Bahkali, Surendra Nimesh
JournalScientific reports (Sci Rep) Vol. 11 Issue 1 Pg. 3824 (02 15 2021) ISSN: 2045-2322 [Electronic] England
PMID33589661 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antineoplastic Agents
  • Drug Carriers
  • Malates
  • Polymers
  • poly-glycerol malate co-dodecanedioate
  • Curcumin
  • Glycerol
Topics
  • Antineoplastic Agents (administration & dosage)
  • Apoptosis (drug effects)
  • Breast Neoplasms (diagnosis, drug therapy, mortality)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Curcumin (administration & dosage)
  • Dose-Response Relationship, Drug
  • Drug Carriers (chemical synthesis, chemistry)
  • Drug Compounding
  • Drug Liberation
  • Female
  • Glycerol (chemical synthesis)
  • Humans
  • Kinetics
  • Malates (chemical synthesis)
  • Nanoparticles (chemistry, ultrastructure)
  • Particle Size
  • Polymers (chemical synthesis)
  • Spectrum Analysis

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